Template:Kyoto/Notebook/Aug 28
From 2013.igem.org
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===Gel Extraction=== | ===Gel Extraction=== | ||
+ | <!-- こっから --> | ||
+ | <div class="experiment"> | ||
+ | <span class="author">No name</span> | ||
+ | {| class="wikitable" | ||
+ | !Lane||DNA | ||
+ | |- | ||
+ | |1||100bpladder||-- | ||
+ | |- | ||
+ | |3||SasA(8/27 Genome PCR production) | ||
+ | |- | ||
+ | |5||RpaA(8/27 Genome PCR production) | ||
+ | |- | ||
+ | |7||RpaB(8/27 Genome PCR production) | ||
+ | |- | ||
+ | |9||PkaiBC(8/27 Genome PCR production) | ||
+ | |} | ||
+ | [[File:igku_xxbeforexx.xxx]]<br> | ||
+ | [[File:igku_xxafterxx.xxx]]<br> | ||
+ | |||
===Colony PCR=== | ===Colony PCR=== | ||
===Restriction Enzyme Digestion=== | ===Restriction Enzyme Digestion=== |
Revision as of 06:08, 21 September 2013
Contents |
Aug 28
Electrophoresis
Miniprep
DNA | concentration[µg/mL] | 260/280 | 260/230 |
---|---|---|---|
8/27 Plux | 173.8 | 1.95 | 1.45 |
Ligation
state | Vector | Inserter | ||
---|---|---|---|---|
experiment | 8/71 DT-1 | 3.0 | 8.0 |
- Samples were evaporeted used evaporator into about 3 µL.
sample | MilliQ | Ligation High | total |
---|---|---|---|
3 | 4 | 3.5 | 10.5 |
- incubate one hour at 16 °C
Gel Extraction
Lane | DNA | |
---|---|---|
1 | 100bpladder | -- |
3 | SasA(8/27 Genome PCR production) | |
5 | RpaA(8/27 Genome PCR production) | |
7 | RpaB(8/27 Genome PCR production) | |
9 | PkaiBC(8/27 Genome PCR production) |
File:Igku xxbeforexx.xxx
File:Igku xxafterxx.xxx